Chimeric cell-targeting pathogenic organism and method of therapeutic use

ABSTRACT

The invention chimeric organism comprises a chimeric surface integrin-like fusion protein in which the I domain has been replaced by an antibody fragment that binds a disease-associated antigen on a cell. Binding of the antibody fragment to the disease-associated antigen triggers virulent transformation of the chimeric pathogenic organism so as to cause the organism to infiltrate the target cell with specificity. Preferably, the chimeric organism is a chimeric pathogenic  C. albicans  having an INT1 fusion protein in which the I domain is replaced by an antibody fragment, preferably a single chain antibody, and in which expression of an iron transporter gene necessary for infiltration of a target cell is triggered under the control of a EFG1p response element. Binding of the antibody to the disease-associated antigen causes filamentous transformation in the chimeric pathogenic  C. albicans  and specific infiltration of target cells. The invention chimeric pathogenic organisms are used in therapeutic methods to specifically infiltrate and destroy diseased cells to which the antibody fragment binds while remaining non-pathogenic to normal cells.

FIELD OF THE INVENTION

[0001] This invention relates to treatment of diseases characterized by production of cell surface markers using antibody-targeted compositions. More particularly, this invention relates to chimeric organisms that express an antibody fragment and to the use of such chimeric organisms in treatment of diseases characterized by production of cell surface markers.

BACKGROUND OF THE INVENTION

[0002] Many recent gene therapy approaches have exploited the specificity of antibody binding to target cancer cell lines in order to deliver either drugs or immune responses to an actual tumor location. Most cancer cell lines misregulate cell surface proteins and polysaccharides, and are thus easily distinguished from normal somal cells by antibodies (R. E. Hawkins et al., Gene Therapy (1998), 5:1581-1583). It is apparent that established carcinomas have successfully avoided activating the immune response within their hosts. Direct attempts to rectify this by recruiting the body's humoral immune response to tumors by injection of murine derived antibodies can unfortunately cause serious and even life threatening human anti-mouse responses (R. K. Jain et al., J Natl. Cancer Inst. (1989) 81:570-576 and D. Colcher et al., J. Natl. Cancer Inst. (1990) 82:1191-1197). In addition, the overall penetration of antibodies into tumors is limited due to the high molecular weights of these molecules (K. A. Chester et al., Adv. Drug Delivery Rev. (1996) 22:303-313).

[0003] In an attempt to limit both the size of the antibody and the mouse-character of the antibody, single chain antibodies (scFvs) that encapsulate the binding features of the Fv region of the antibody without the bulk of the native antibody sequence in the c1, c2, and c3 domains have been developed. One methodology to generate scFvs involves tethering the antigen binding domains of V_(H) and V_(L) together using a short flexible peptide linker (R. E. Bird et al., Science (1988) 242:423-426). Another approach involves the generation de novo of molecular diversity, instead of generating monoclonal antibodies in mice. By using combinatorial antibody libraries on the surface of filamentous bacteriophage screened against immobilized antigen, a single polypeptide chain that is amenable to fusion with other proteins can be generated (J. S. Huston et al., Proc. Natl. Acad. Sci. USA (1988) 85:5879-5883; J. McCafferty, Nature (1990) 348:552-554; R. H. J. Begent et al., Nature Med. (1996) 2:979-984, reviewed in K. A. Chester et al., Adv. Drug Delivery Rev. (1996) 22, 303-313). The scFvs obtained by either methodology above show better tumor penetration, but therapeutic application is still in early stages (G. Reitmuller et al., Lancet (1994) 343:1177-1183). However, fusions between imaging agents and scFvs have found wide acceptance and extensive application in tumor imaging and radiochemotherapeutic delivery (see J. Bhatia et al., Cancer (1999) 85:571-577 and A. M. Wu et al., Tumor Targeting (1999) 4:47-58 and references therein).

[0004] Antibody recognition has also been used to target cancer cells by incorporation of an scFv into the envelope protein of a retrovirus (S. J. Russell et al., Nuc. Acids Res. (1993) 21:1081-1085 and F. Martin et al., Human Gene Therapy (1998) 9:737-746). This targeting is modest, but offers some promise, as has been demonstrated for certain types of melanoma (Martin 1998). In addition, adenovirus infection has been used to allow the transient expression of tumor-targeting scFv fusion proteins in whole organisms with moderate success (H. A. Whittington et al., Gene Therapy (1998) 5:770-777). Unfortunately, low survivability of adenoviruses carrying antibody generating expression vectors limits their impact.

[0005] The most promising therapeutic techniques relying on the specificity of antibody binding focus on engineering T-cells that express antibody fragments fused to surface proteins, and are thus directed to tumor surfaces (recent work reviewed in F. Paillard, Human Gene Therapy (1999) 10:151-153). Some of these T-cells are at present in clinical trials. Strategies used to date, however, have drawbacks, including limited efficacy against established tumors, though demonstrating some slowing of tumor metastasis (R. P. McGuinness et al, Human Gene Therapy (1999) 10:165-173). Limited effectiveness against established tumors may be due to the inability of the T-cells to penetrate solid cell masses (Paillard 1999). True protection against establishment of invasive carcinoma was obtained only by coinjection of modified T-cells with the tumorogenic line. In clinical applications, this may permit stabilization and localization of established tumors, but not reductive treatment. Another potential problem is that suicide signals T-cells use to induce apoptosis, like tumor necrosis factor I, are often not functional against carcinomas. Even when they are effective, successful cancer cell lines will rapidly adapt to apoptotic signals, and have even been known to induce apoptosis in attacking T-cells (K. Shiraki, Proc. Natl. Acad. Sci. USA (1996) 94:6420-6425). In addition, T-cells bearing these chimeras are assembled separately for each patient ex vivo due to possible MHC incompatibilities that could result in serious allergic reactions were T-cells from other humans introduced therapeutically.

[0006]Candida albicans is the most commonly isolated invasive fungal pathogen in humans. This organism is representative of several that switch between two major classes of morphology. The first morphology is the ellipsoid blastospore. Like most yeast, C. albicans assumes this architecture when growing non-pathogenically. Upon binding of C. albicans to mammalian tissues (i.e. via the I domain of the INT-1 protein), the cell morphology switches to various filamentous forms, including germ tubes and hyphae, that are capable of aggressively invading host tissue (reviewed by R. A. Calderone, Microbol. Rev. (1991) 55, 1-20). Systemic infection of a vulnerable host by C. albicans results in high levels of mortality. For example, more than 30% of immunocompromised HIV patients are systemically infected despite appropriate treatment regimes. In addition, C. albicans infection commonly leads to death in premature infants, diabetics, and surgical patients. To date, the ability of this pathogenic organism to infect cells when the cell morphology switches to a filamentous form has not been utilized for therapeutic purposes, such as in cancer therapy.

[0007] Thus, the need exists in the art for new and better compositions and methods of their use for treating various types of cancers and other diseases associated with production of an abnormal protein.

SUMMARY OF THE INVENTION

[0008] The present invention overcomes these and other problems in the art by providing chimeric organisms having a chimeric surface integrin-like protein in which the I domain has been replaced by an antibody fragment that binds a disease-associated antigen on a cell. Binding of the antibody fragment to the disease-associated antigen on the cell triggers virulent transformation of the chimeric pathogenic organism and allows the organism to infect the cell.

[0009] In one embodiment according to the present invention, there are provided chimeric pathogenic C. albicans modified to contain an integrin1 (INT1) fusion protein in which the I domain is replaced by an antibody fragment that binds to a disease-associated antigen on a diseased cell. The chimeric C.albicans further contains a disabled wild-type high affininity iron transporter (CAFTR) gene, and a DNA construct comprising a wild-type CAFTR gene under the control of an enhanced filamentous growth protein (EFG1p) response element, wherein binding of the antibody to the disease-associated antigen triggers expression of the CAFTR gene in the DNA construct and filamentous transformation in the chimeric pathogenic C. albicans.

[0010] In another embodiment according to the present invention, there are provided methods for treating a disease associated with the presence of cells having a disease-associated surface antigen in a subject in need thereof by administering to the subject a therapeutically effective amount of an invention chimeric pathogenic organism so as to cause binding of the antibody fragment to the disease-associated antigen on the cells, thereby treating the disease by triggering infiltration of the chimeric pathogenic C. Albicans into the cells without substantial damage to healthy cells.

[0011] In yet another embodiment, the present invention provides methods for generating a chimeric therapeutic organism from a pathogenic organism that possesses in the wild-type an integrin-like protein with an I domain. In the invention methods, the I domain in the integrin-like protein of the pathogenic organism is replaced with an antibody fragment that binds to a disease-associated antigen on a diseased cell. In the chimeric therapeutic organism, virulent transformation occurs upon binding of the antibody fragment to the disease-associated antigen on the cell.

A BRIEF DESCRIPTION OF THE DRAWINGS

[0012] FIGS. 1A-W show the nucleotide sequence of the gene that encodes the integrin-like INT1 protein of C. albicans (GenBank Accession # U35070) (SEQ ID NO:1)

[0013]FIG. 2 shows the nucleotide sequences of seven primers used in construction of the chimeric C. albicans of Example 1 (SEQ ID NOS:2 through 8, respectively).

[0014]FIG. 3 is a schematic drawing showing human integrin structure (adapted from M. J. Humphries, Biochem. Soc. Trans. (2000) 28:311-340).

[0015]FIG. 4 is a schematic drawing showing two pathways by which hyphal development in yeast is regulated.

DETAILED DESCRIPTION OF THE INVENTION

[0016] The present invention provides chimeric pathogenic organisms derived from wild type organisms wherein virulent transformation of the organism is controlled in the wild-type organism by binding of the I domain of a surface integrin-like protein to a cell. The invention chimeric organism comprises a chimeric surface integrin-like protein in which the I domain is replaced by an antibody fragment that binds a disease-associated antigen on a cell. Binding of the antibody fragment to the disease-associated antigen triggers virulent transformation of the chimeric pathogenic organism so as to cause the organism to infiltrate the cell. Virulent invasion of the cell by the chimeric pathogen inhibits growth of the diseased cell.

[0017] The invention pathogenic chimeric organism represents a new approach to employing otherwise pathogenic organisms to assist in disease treatment. Although the present invention is described for illustrative purposes with reference to a reingeneered C albicans, suitable pathogenic organisms in addition to C. albicans that can be engineered according to the methods disclosed herein are pathogenic organisms that become virulent (e.g., switch to a filamentous invasive form) upon binding of its integrin-like surface protein (i.e., a cell-cell communication protein) to a target on another cell and in which the binding domain of the surface protein can be replaced with a antibody fragment that binds to a desired target cell associated with a disease state. Preferably the chimeric pathogen also is relatively harmless to mammalian cells until binding of the antibody fragment contained in its surface protein.

[0018] In higher eukaryotes, integrins are one of the most important classes of surface proteins responsible for intercellular communication (reviewed in F. G. Giancotti Science (1999) 285:1028-1032 and M. J. Humphries, Biochem. Soc. Trans. (2000) 28:311-340). Generally, integrins are heterodimers, each subunit of which consists of a cytosolic domain with one tyrosine used as a kinase regulatory site, a transmembrane domain, and four EFG-like repeats. As used herein, the term “integrin-like protein” refers to a cell-cell communication transmembrane protein that contains one or more of the above features.

[0019] There are various other domains on the integrin proteins, including metal binding MIDAS loops and β propeller domains. Notably, in nine of the fifteen human integrin I subunits, there is a protruding region known alternately as the IA, or the I domain, which appears to regulate integrin targeting. This suggests that the absence or presence of the I domain has little, if any, effect on the integrin's ability to transduce signals, but instead regulates which signals are transduced. The I domain is the only region whose structure has been solved crystallographically (both bound to its target proteins and unbound). Based on these studies, it is believed that the I domain alone is indeed sufficient for binding to collagen (J. Emsley Cell (2000) 101:47-56).

[0020] In the invention chimeric organism, the endogenous binding region of the surface integrin-like protein, which nonspecifically targets cells (e.g., those containing fibrinogen), is replaced with an antibody fragment, such as a single chain antibody. As a result, rather than nonspecifically binding to any cell containing a binding site for the endogenous binding region, the invention chimeric pathogen binds with specificity to cells that express the target antigen. Binding of the chimeric pathogen to a cell containing an epitope for the antibody fragment triggers virulent invasion of the disease-associated cell. Other cells (e.g., healthy cells) are not bound by the chimeric organism. As a result, pathogenic infiltration of non-targeted cells does not take place.

[0021] In one embodiment, the invention provides a chimeric pathogenic C. albicans comprising an INT1 fusion protein in which the I domain is replaced by an antibody fragment that binds to a disease-associated antigen on a cell. Preferably, the INT1 protein in the invention pathogenic organism is a fusion protein in which a single chain antibody replaces the native I domain. The nucleotide sequence encoding INT1 is shown in FIGS. 1A-W (SEQ ID NO:1 herein). Construction of such a chimeric INT1 is described in Example 1 below.

[0022] As used herein, the term “disease-associated antigen” means either that the antigen is not expressed in normal, healthy cells, or that the antigen is expressed in abnormal quantity in diseased cells. Existence of disease-associated antigen on cells greatly increases the amount of the chimeric pathogen that attacks such disease-associated cells.

[0023] Preferably the antibody fragment is a single chain antibody (scFv), ), but Fv and CDR fragments can also be used. The antibody fragment is preferably incorporated into the surface integrin-like protein to form a fusion protein.

[0024] In a preferred embodiment, the chimeric pathogen is a chimeric Candida albicans, the most common fungal pathogen of humans. In immunocompromised individuals, C. albicans is a dangerous, and sometimes lethal pathogen. The primary protein responsible for C. albicans targeting is an integrin-like transmembrane protein known as INT1. INT1 contains an integrin-like domain (known as the I domain), which is the putative targeting region of this protein. FIGS. 1A-W show the nucleotide sequence of the gene that encodes the integrin-like INT1 protein of C. Albicans (GenBank Accession # U35070) (SEQ ID NO:1).

[0025] The preferred antibody fragment for incorporation into the INT1 protein as a fusion protein is a single chain antibody (scFv), but Fv and CDR fragments can also be used. Thus, in this embodiment, the power and specificity of scFv antibody fragments, which now exist against a considerable number of cell surface targets in cancer cell lines, is combined with the ability to not only bind to the cancer cell mass, but to invade and destroy tumors aggressively and selectively in a manner independent and complementary to the body's own defenses.

[0026] The present invention exploits the mechanism involved in the filamentous transformation of C. albicans and similar pathogenic organisms, which is controlled by a regulatory system similar to that used by Saccharomyces cerevisiae to alter its own morphology under nitrogen starvation conditions and agar invasive conditions. The evolutionary conservation of this pathway has greatly facilitated deconvoluting the biochemistry involved, and recent research has resulted in a better understanding of proteins responsible for C. albicans intercellular binding and pathogenicity. In particular, INT1 is the previously known but unidentified surface protein that is strongly crossreactive with antibodies for certain leukocyte integrins, and appears to be the primary protein responsible for attaching to target cells (C. A. Gale et al., Science (1998) 279:1355-1358). INT1 is a transmembrane surface protein isolated by cDNA screening of the C. albicans genome by oligonucleotide probes derived from the conserved region of human integrins (C. Gale et al., Proc. Natl. Acad. Sci. USA (1996) 93:357-361). Over the last fifteen years, many reports have appeared in the literature describing surface proteins that are related to I-subunits of the leukocyte integrins IM/l2 (Mac-1; CD11b/CD18) and IX/l2 (p150,95; CD11c/CD18) (C. M. Bendel, J. Clin Invest. (1993) 92:1840-1849 and references therein). Many monoclonal antibodies that recognize epitopes of these leukocyte surface proteins cross react to blastospores and germ tubes of C. albicans, sometimes with the same affinity as to the original human targets.

[0027] Upon ligand binding, INT1 signals cell morphology changes that induce hyphae growth. This signaling pathway appears to be largely independent of the mating factor MAPK pathway, which is most commonly associated with morphologic changes. Unlike the pathway that is triggered by ligand binding, the MAPK pathway is triggered by environmental stimulation, such as changes in pH, temperature, mating signaling or nutrient availability, and terminates in transcription factor STE12 in S. cerevisiae (Gale 1996; C. J. Gimeno et al., Cell (1992) 68, 1077-1090 1992 and R. L. Roberts et al., Genes Dev. (1994) 8, 2974-2985) (FIG. 4).

[0028] The second pathway to hyphal morphology, which is less well characterized, depends on direct stimulation by serum. Addition of mammalian serum to an otherwise spheroplast culture of C. albicans induces hyphae growth, even when the signaling cascade terminating in STE12 (briefly described above) is completely knocked out (Lo 1997). INT1 instead communicates morphology changes via a second, STE12 independent, pathway that appears to have as an intermediary protein Ash1. Ash 1 is a daughter cell-specific protein that helps regulate filamentous growth, and may interact with STE20 (S. Chandarlapaty et al., Mol. Cell Biol. (1998) 18, 2884-2891). This pathway terminates at the transcriptional level in a bHLH class protein known as PHD1 recently isolated in S. cerevisiae. The homologous protein in C. albicans is known as EFG1. The sequence for EFG1 is fully described in W. R. Stoldt et al., EMBO Journal (1997) 16, 1982-1991, which is incorporated herein by reference in its entirety.

[0029] For both S. cerevisiae and C albicans, overexpression of their respective analog is sufficient to induce hyphae growth (Stoldt 1997). Importantly, elimination of filamentous growth can only be achieved after disabling both of these two pathways. This observation also rules out a third pathway for signaling.

[0030] In construction of the illustrative C. albicans chimeric pathogen, the integrin homolog INT1 was isolated using conserved transmembrane sequences from mammalian integrins to clone the cDNA copy of the gene in C. albicans. Removal of the INT1 protein reduces specific adhesion of C. albicans to HeLa cells by 39%. Therefore, though INT1 is a critical protein for binding to a target, other proteins as well must serve to help mediate this interaction (vide infra), though these proteins have yet to be identified. Still, previous research appears to be consistent with cell surface binding by a single, integrin-like protein of approximate MW of 165 kDa. Interestingly, transgenic experiments where INT1 was overexpressed on the surface of Saccharomyces cerevisiae, a nonadhesive and nonpathogenic species, caused strong adhesion to mammalian cells. Thus, INT1 alone is sufficient for target binding.

[0031] Deletion of the INT1 gene cripples filamentous growth of Candida, though not entirely eliminating it. It has been shown that invasive growth of this type is necessary for parasitic microorganisms to successfully invade host tissues (W-S Lo et al., Mol. Biol. Cell (1998) 9:161-171). In vivo testing of the pathogenicity of an INT1 of pathogenicity of the INT1 deletion strain of C. albicans on mice was conducted and showed a dramatic reduction in mouse lethality compared to wild-type strains (Gale 1996).

[0032] The similarity of INT1 in C. albicans to mammalian integrins is not limited to antibody cross reactivity and sequence similarity in the transmembrane region. Notably, INT1 also appears to contain numerous motifs similar by homology to mammalian integrin motifs. These include (1) two FE-hand divalent cation binding sites that likely mediate target binding; (2) a single cytosolic tyrosine for kinase signaling; and, most importantly, (3) a region that appears to be homologous to the I domain of integrins. Similar to the higher mammalian IM and IX that recognize iC3b and fibrinogen, the I domain like region in C. albicans INT1 is generally thought to be the binding site that targets iC3b. This is further supported by its ˜25% sequence identity with the fibrogen binding domain of Staphylococcus aureus.

[0033] In the illustrative preferred embodiment of the invention chimeric pathogen, the I domain of the wild-type INT1 protein, which nonspecifically targets fibrinogen, is replaced with an scFv that targets cancer cells. Many scFvs already have been developed that bind to a wide variety of tumor cells for therapeutic applications. Such studies take advantage of the severe misregulation of surface protein populations in tumors by utilizing scFvs that bind epitopes found in such surface proteins. For example, therapeutic applications involving T-cell, viral, and/or drug targeting has already been proven in vivo using scFvs shown in Table I below. TABLE 1 CANCER LINE ANTIBODY ANTIGEN AND LOCATION REFERENCES OTHER CC49 TAG-72 Adenocarcinoma McGuiness 1999 (colon, Shu 1993 ovarian, breast) Kashmiri 1995 FRP5 ERBB2 Breast, ovarian Moritz 1994 Previously used to Harwerth 1992 construct cytotoxic Hynes 1993 C-lymphocytes. Also used to direct virus targeting (Galmiche 1997) GA733.2 EGP-2 Various Ren-Heidenreich 2000 HMN-14 CEA Colorectal, breast, Nolan 1999 Previously used to pancreas, other construct killer T-cells VFF17 CD44 Cervical cancer, Dall 1997 lymph metastases Hekele 1996 MOV19 I-FR Nonmucinous ovarian Melani 1998 carcinoma 7.16.4 Neu Breast Katsumata 1995 Antigen (neu) is same Stankovski 1993 as ERBB2, and is Disis 1997 protein bound by Herceptin. MLuCl L(Y) TAA Various Mezzanzanica Targets misregulated 1998 carbohydrates. Lewis (Y) tumor associated antigen

[0034] By replacing the I domain in the integrin-like surface protein with a scFv that binds to a disease-associated tumor cell, the invention chimeric pathogenic organisms are engineered to take advantage of the severely misregulated production of surface protein populations in tumors. In the present invention, the antibody fragment, preferably as a scFv, is incorporated into the position of the native binding domain of an integrin-like protein (i.e., the creation of a fusion protein that contains the scFv incorporated in the place of the I domain in the wild-type pathogenic organism). Many antibody fragments have already been tested for selective binding to a known tumor-associated antigen, for example, as shown in Table 1. Representative nonlimiting examples of tumor associated antigens to which scFvs of the invention chimeric pathogens bind include GAG-72, ERBB2, EGP-2, CEA, CD44, I-FR, neu, the Lewis (Y) tumor associated antigen, and the like.

[0035] As used herein, the terms “disease- or tumor-associated antigen” and “disease- or tumor-associated epitope” encompass antigens and epitopes, respectively, found in surface proteins produced in large amounts in various types of tumors as well as various types of marker proteins (and the epitopes contained therein) that are found associated with tumor cells and not found associated with normal cells. Representative non-limiting examples of tumors having associated antigens to which antibody fragments (e.g., scFvs) of the invention chimeric pathogens bind includes adenocarcinoma of colon, ovary or breast; cervical cancer, nonmucinous ovarian carcinoma; breast, ovarian, colorectal, and pancreatic cancer, and the like. Invention chimeric pathogenic organisms are incapable of infiltrating a cell in the subject until the antibody fragment in the chimeric integrin-like protein binds to its target epitope, triggering a virulent transformation of the chimeric pathogenic organism. Therefore, the invention chimeric pathogenic organisms are substantially incapable of pathogenic activity, such as infiltration, of cells other than their target cells (e.g., cancer cells).

[0036] Preferably, the antibody fragment is a scFv and is introduced in the place of the I domain of INT-1 in C. albicans. Once engineered to replace the wild-type binding domain of the INT1 protein with an antigen binding region (e.g. scFv) from cancer-specific antibodies, the invention mutant C. albicans strain will specifically bind to a cancer line dictated by the targeting of the scFv-INT1 fusion protein.

[0037] Optionally, in order to direct pathogenicity specifically to the target cell (e.g., a carcinoma cell) a gene in the pathogenic organism from which the chimeric organism is derived that is required for invasive growth is disabled or removed and a DNA construct comprising a reengineered copy of the gene necessary for invasive growth is introduced into the chimeric organism under the regulatory control of a transcription factor that regulates filamentous transformation of the organism. However, the gene removed should be one that does not significantly affect vegetative growth of the organism so that large quantities of this chimeric organism can be produced using standard culture techniques.

[0038] For example, in C albicans, the wild-type gene is placed under the control of a EFG1p response element. While the CaFTR1 gene is currently preferred for reengineering in C. albicans, those of skill in the art can readily substitute for reengineering (i.e., in the place of the CaFTR1 gene) another gene from the pathogenic organism that is essential or preferred for pathogenic invasion.

[0039] Preferably, in the invention chimeric C. albicans, the wild-type CAFTR gene is either disabled or removed and a DNA construct comprising a wild-type CAFTR gene under the control of a EFG1p response element is introduced. Overexpression of EFG1 in C. albicans leads to enhanced filamentous growth in liquid and on solid media. Overexpression of EFG1 by a PCK1p-EFG1 fusion is described by A. Sonneborn, Infect Immun (1999) 67:9:4655-60, which is incorporated herein by reference in its entirety (See also, V. R. Stoldt et al., EMBO J (1997) 16:8 1982-91). The nucleotide sequence for the CaFTR1 gene of C. albicans is found at NCBI GenBank Number AF195775.

[0040] CaFTR1 extracts iron from mammalian tissues that withhold metals from microbial predators as a defense mechanism (D. M. DeSilva et al., Physiol. Rev. (1996) 76, 31-47 and H. Gunshin et al., Nature (1997) 388, 482-488). Removal of the native CaFTR1 completely abrogates pathogenicity. Mice injected with a mutant C. albicans having a disabled CaFTR1 gene survive entirely; while those injected with an equal amount of wild-type C. albicans do not. Under circumstances of normal unicellular growth in an abundance of iron, though, CaFTR1 is not an essential gene. In conditions where iron is in limited quantities, for instance during circulation through a host designed to have limiting nutrient levels, this gene is highly upregulated. Removal of the CaFTR1 gene only causes a growth (and thus invasion) deficiency when pathogenesis is initiated. This protein is normally regulated entirely independently from the morphology signaling pathway, and its concentration is dependent only on the heavy metals detected in the environment. By placing this protein under the transcriptional control of the cell morphology pathway initiated by INT1, as described herein, the pathogenicity of the overall assembly can be tightly restricted to scFv-INT1 targeted cells.

[0041] In this preferred embodiment of the invention chimeric pathogenic organism, binding of the antibody to the disease-associated antigen triggers both expression of the CAFTR gene in the DNA construct and filamentous transformation of the chimeric pathogenic C. albicans. Since expression of INT1 in wild-type C. albicans is activated by INT1 binding to other cells, placing expression of the C. albicans iron transporter under control of the Efg1 expression system ensures that both the pathogenicity and the binding of the invention chimeric organism is directed specifically to target cells. If the antibody fragment incorporated in the place of the INT1 binding domains is specific for a tumor cell, the pathogenicity of the C. albicans cell line is directed specifically towards target cancerous cells, and nonspecific toxicity is inhibited. In other words, the virulence of the engineered strain of C. albicans will only be activated once scFv-INT1 binds to its target antigen on the surface of the carcinoma.

[0042] The gene that triggers filamentous growth can be disabled in the invention chimeric organism using any method known in the art, for example, by disruption of the gene at both diploid loci using standard techniques. The native gene can be reintroduced under the control of a response element (e.g., a transcription factor) that regulates filamentous transformation of the organism using known techniques, such as by use of homologous recombination (as described in Example 1 herein). This regulatory reassignment of the gene that triggers transformation tightly limits the pathogenicity dependent on this protein to the specified target.

[0043] In yet another embodiment, the present invention provides methods for treating a disease associated with the presence of cells having a disease-associated surface antigen in a subject in need thereof. The invention method includes administering to the subject, a therapeutically effective amount of an invention chimeric pathogenic organism so as to cause binding of the antibody fragment to the disease-associated antigen on the cell, thereby specifically treating the disease by triggering infiltration of the chimeric pathogenic organism into the cells without substantial damage to healthy cells. The invention method may further include administering to the subject an immunosuppressive agent to inhibit the subject's immune system from destroying the chimeric pathogen prior to achieving a therapeutic effect. Representative immunosuppressive agents useful in the practice of the invention methods include such agents as cyclosporin A, OKT3, FK506, mycophenolate mofetil (MMF), azathioprine, corticosteroids (such as prednisone), antilymphocyte globulin, antithymocyte globulin, and the like. In a preferred embodiment of the invention methods, the invention chimeric pathogen is used to target and attack tumor cells.

[0044] In invention therapeutic methods, the chimeric pathogenic organisms are used to infiltrate and destroy both ex vivo cell lines (e.g., tumor cell lines), as well as in vivo murine models of human carcinomas, and the like. The invention pathogenic organisms also have specific utility as research reagents for the testing of therapeutic compositions. For example, the invention chimeric organisms can be used to compare the therapeutic effect against a particular cell line of various antibody fragments engineered into the surface integrin-like protein. Binding of invention organisms to these ex vivo and in vivo models can be tested for efficacy using known assays (e.g., mouse tumor models) to determine binding of the antibody fragment (e.g., single chain antibody) to the target antigen on a disease-associated cell.

[0045] The chimeric pathogens used in practice of the invention method can be administered for therapeutic purposes, such as treatment of tumor, by any route known to those of skill in the art, such as intraarticularly, intracisternally, intraocularly, intraventricularly, intrathecally, intravenously, intramuscularly, intraperitoneally, intradermally, intratracheally, intracavitarily, and the like, as well as by any combination of any two or more thereof.

[0046] The most suitable route for administration will vary depending upon the disease state to be treated, or the location of the suspected condition or tumor to be treated. For example, for treatment of inflammatory conditions and various tumors, local administration, including administration by injection directly into the body part containing the tumor provides the advantage that the chimeric pathogen can be administered in a high concentration without risk of the complications that may accompany systemic administration thereof.

[0047] The chimeric pathogen is administered in “a therapeutically effective amount.” An effective amount is the quantity of a chimeric pathogen necessary to aid in treatment, inhibition or destruction of diseased tissue (e.g. tumor) under treatment in a subject. A “subject” as the term is used herein is contemplated to include any mammal, such as a domesticated pet, farm animal, or zoo animal, but preferably is a human. Amounts effective for therapeutic use will, of course, depend on such factors as the size and location of the body part to be treated, the affinity of the antibody fragment for the target antigen, the type of target tissue, as well as the route of administration. Local administration of the targeting construct will typically require a smaller dosage than any mode of systemic administration, although the local concentration of the chimeric pathogen may, in some cases, be higher following local administration than can be achieved with safety upon systemic administration.

[0048] The invention composition can also be formulated as a sterile injectable suspension according to known methods using suitable dispersing or wetting agents and suspending agents. The sterile injectable preparation may also be a sterile injectable solution or suspension in a nontoxic parenterally-acceptable diluent or solvent, for example, as a solution in 1-4, butanediol. Sterile, fixed oils are conventionally employed as a solvent or suspending medium. For this purpose any bland fixed oil may be employed, including synthetic mono- or diglycerides, fatty acids (including oleic acid), naturally occurring vegetable oils like sesame oil, coconut oil, peanut oil, cottonseed oil, etc., or synthetic fatty vehicles like ethyl oleate, or the like. Buffers, preservatives, antioxidants, and the like, can be incorporated as required, or, alternatively, can comprise the formulation.

[0049] Preferably the antibody fragment is a scFv incorporated into the chimeric surface protein of the pathogen as a targeting device and is not relied upon as the toxic agent. Rather, it is the pathogenic organism itself that invades and destroys the target cells in accordance with the present invention. A single chain antibody (scFv) is a genetically engineered molecule containing the variable region of the light chain and the variable region of the heavy chain, linked by a suitable polypeptide linker as a genetically fused single chain molecule. Methods of making these fragments are known in the art. (See for example, Harlow & Lane, Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory, New York, 1988, incorporated herein by reference). As used in this invention, the term “epitope” means any antigenic determinant on an antigen to which the paratope of an antibody binds. Epitopic determinants usually consist of chemically active surface groupings of molecules such as amino acids or sugar side chains and usually have specific three-dimensional structural characteristics, as well as specific charge characteristics.

[0050] Fv fragments comprise an association of V_(H) and V_(L) chains. This association may be noncovalent, as described in Inbar et al., Proc. Nat'l Acad. Sci. USA 69:2659, 1972. Alternatively, the variable chains can be linked by an intermolecular disulfide bond or cross-linked by chemicals such as glutaraldehyde. See, e.g., Sandhu, Crit. Rev. Biotech. 12:437, 1992; and Singer et al., J. Immunol. 150:2844, 1993. Preferably, the Fv fragments comprise V_(H) and V_(L) chains connected by a peptide linker. These single-chain antigen binding proteins (scFv) are prepared by constructing a structural gene comprising DNA sequences encoding the V_(H) and V_(L) domains connected by an oligonucleotide. The structural gene is inserted into an expression vector, which is subsequently introduced into a host cell such as E. coli. The recombinant host cells synthesize a single polypeptide chain with a linker peptide bridging the two V domains. Methods for producing scFvs are described, for example, by Whitlow et al., Methods: a Companion to Methods in Enzymology, 2: 97, 1991; Bird et al., Science 242:423-426, 1988; Pack et al., Bio/Technology 11:1271-77, 1993; Sandhu, supra, and Ladner et al., U.S. Pat. No. 4,946,778, which is hereby incorporated by reference in its entirety.

[0051] Another form of an antibody fragment suitable for incorporation as a fusion protein in invention chimeric pathogenic organisms is a peptide coding for a single complementarity-determining region (CDR). CDR peptides (“minimal recognition units”) can be obtained by constructing genes encoding the CDR of an antibody of interest. Such genes are prepared, for example, by using the polymerase chain reaction to synthesize the variable region from RNA of antibody-producing cells. See, for example, Larrick et al., Methods: a Companion to Methods in Enzymology, 2: 106, 1991.

[0052] Antibodies that bind to a tumor cell or other disease-associated antigen can be prepared using an intact polypeptide or biologically functional fragment containing small peptides of interest as the immunizing antigen. The polypeptide or a peptide used to immunize an animal (derived, for example, from translated cDNA or chemical synthesis) can be conjugated to a carrier protein, if desired. Commonly used carriers that are chemically coupled to the peptide include keyhole limpet hemocyanin (KLH), thyroglobulin, bovine serum albumin (BSA), and tetanus toxoid, and the like. The coupled peptide is then used to immunize the animal (e.g., a mouse, a rat, or a rabbit).

[0053] The preparation of such monoclonal antibodies is conventional. See, for example, Kohler & Milstein, Nature 256:495, 1975; Coligan et al., sections 2.5.1-2.6.7; and Harlow et al., in: Antibodies: a Laboratory Manual, page 726 (Cold Spring Harbor Pub., 1988), which are hereby incorporated by reference. Briefly, monoclonal antibodies can be obtained by injecting mice with a composition comprising an antigen, verifying the presence of antibody production by removing a serum sample, removing the spleen to obtain B lymphocytes, fusing the B lymphocytes with myeloma cells to produce hybridomas, cloning the hybridomas, selecting positive clones that produce antibodies to the antigen, and isolating the antibodies from the hybridoma cultures. Monoclonal antibodies can be isolated and purified from hybridoma cultures by a variety of well-established techniques. Such isolation techniques include affinity chromatography with Protein-A Sepharose, size-exclusion chromatography, and ion-exchange chromatography. See, for example, Coligan et al., sections 2.7.1-2.7.12 and sections 2.9.1-2.9.3; Barnes et al., Purification of Immunoglobulin G (IgG), in: Methods in Molecular Biology, Vol. 10, pages 79-104 (Humana Press, 1992).

[0054] Antibodies of the present invention may also be derived from subhuman primate antibodies. General techniques for raising therapeutically useful antibodies in baboons can be found, for example, in Goldenberg et al., International Patent Publication WO 91/11465 (1991) and Losman et al., 1990, Int. J. Cancer 46:310, which are hereby incorporated by reference. Alternatively, a therapeutically useful antibody may be derived from a “humanized” monoclonal antibody. Humanized monoclonal antibodies are produced by transferring mouse complementarity determining regions from heavy and light variable chains of the mouse immunoglobulin into a human variable domain, and then substituting human residues in the framework regions of the murine counterparts. The use of antibody components derived from humanized monoclonal antibodies obviates potential problems associated with the immunogenicity of murine constant regions. General techniques for cloning murine immunoglobulin variable domains are described, for example, by Orlandi et al., Proc. Nat'l Acad. Sci. USA 86:3833,1989, which is hereby incorporated in its entirety by reference. Techniques for producing humanized monoclonal antibodies are described, for example, by Jones et al., Nature 321:522, 1986; Riechmann et al., Nature 332:323, 1988; Verhoeyen et al., Science 239:1534, 1988; Carter et al., Proc. Nat'l Acad. Sci. USA 89:4285, 1992; Sandhu, Crit. Rev. Biotech. 12:437, 1992; and Singer et al., J. Immunol. 150:2844, 1993, which are hereby incorporated by reference.

[0055] It is also possible to use anti-idiotype technology to produce monoclonal antibodies, which mimic an epitope. For example, an anti-idiotypic monoclonal antibody made to a first monoclonal antibody will have a binding domain in the hyper variable region that is the “image” of the epitope bound by the first monoclonal antibody.

[0056] The assembly, selection, and integration of these chimeric scFv-INT1 products are conducted using standard molecular biology, for example as is described in Example 1 herein. The proper assembly of the invention chimeric scFv-INT-1 protein and adhesion to the epitopes in target cell lines, e.g., tumor cell lines, can be tested by introduction of the chimeric assembly into S. cerevisiae, preferably under the control of a promoter, such as the actin promoter, that is constantly activated in such yeast cell lines. Yeast cells (e.g., Saccharomyces cerevisiae) possess an efficient and precise system for genetic recombination. The natural process of homologous recombination depends on a system of enzymes that search for regions of sequence homology between two DNA molecules (which may be entire chromosomes). Once homology is found, an exchange of information is possible.

[0057] Plasmids or other vectors carrying recombinant-DNA (r-DNA) clones which contain naturally-occurring yeast sequences and which are introduced into cells by standard transformation methods are capable of stably integrating into the yeast genome at sites of homology. The efficiency of this process can be increased by up to a thousand-fold by introducing a double-strand break within a DNA sequence on the incoming DNA molecule that is homologous to a sequence resident in the yeast cell. The cloned yeast DNA on the transforming vector is referred to herein as the targeting sequence, and the site of integration is referred to herein as the target site.

[0058] In one process described in U.S. Pat. No. 5,783,385 to Treco , et al., which is incorporated herein by reference in its entirety, a targeting DNA molecule, e.g., a bacterial plasmid, which is non-replicating in yeast is introduced into the population of host yeast cells containing the r-DNA. The bacterial plasmid has a selectable marker gene that functions in yeast and a first targeting DNA sequence which is homologous in part to a second target r-DNA clone sequence. Preferentially, the targeting plasmid is cut with a restriction endonuclease that introduces a double-strand break within the targeting sequence, thereby linearizing the bacterial plasmid and providing DNA ends which are recombinogenic to stimulate the process of homologous recombination with host yeast sequences. Because the plasmid is non-replicating in yeast, stable transformation with the selectable marker can only proceed by homologous recombination. The efficiency of transformation by homologous recombination is increased when the plasmid is cut by restriction enzyme digestion within the targeting DNA sequence homologous in part to the target r-DNA sequence.

[0059] The host yeast cells are grown under conditions such that only those yeast cells that have been stably transformed, i.e., have had the plasmid and selectable marker stably integrated in the host cell by homologous recombination will be able to grow. In a correctly targeted event, the entire plasmid is stably incorporated contained in the host yeast cell by homologous recombination of the targeting DNA sequence of the plasmid and the homologous target r-DNA clone sequence. Only those few host yeast cells that contain the desired, target r-DNA clone sequence (and have thereby undergone homologous recombination with the targeting plasmid) are able to grow under the new growth conditions, due to the introduction of the yeast-selectable marker gene contained on the targeting plasmid.

[0060] The vast majority of the population of the host yeast cells containing r-DNA clone sequences that are not homologous to the targeting DNA sequence contained on the plasmid, do not have the plasmid incorporated by homologous recombination and, therefore, do not acquire the marker gene that is essential for growth under the selection conditions. Therefore, it is preferable that any yeast-selectable marker gene that is contained on the incoming targeting plasmid has been deleted entirely or almost entirely from the genome of the host yeast strain that is used for the vector. This prevents any spurious homologous recombination events between the incoming yeast-selectable marker gene and any other natural yeast genetic loci. If a yeast-selectable marker gene on the incoming targeting plasmid is not deleted from the yeast genome, but is retained as a mutated, non-functional portion of the yeast chromosome, more positive scores for homologous recombination will have to be screened to ensure that the homologous recombination event has taken place between the targeting DNA sequence on the bacterial plasmid and the desired, target r-DNA clone sequence. Cells with the integrated marker can grow into colonies when plated on appropriate selective media.

[0061] Alternatively, a yeast-selectable marker gene on the incoming targeting DNA molecule can be a bacterial gene that confers drug resistance to yeast cells, e.g., the CAT or neo genes from Tn9 and Tn903, or bacterial amino acid or amino acid nucleoside prototrophy genes, e.g., the E. coli argH, trpC, and pyrF genes.

[0062] Methods for plasmid purification, restriction enzyme digestion of plasmid DNA and gel electrophoresis, use of DNA modifying enzymes, ligation, transformation of bacteria, transformation of yeast by the lithium acetate method, preparation and Southern blot analysis of yeast DNA, tetrad analysis of yeast, preparation of liquid and solid media for the growth of E. coli and yeast, and all standard molecular biological and microbiological techniques can be carried out essentially as described in Ausubel et al. (Ausubel, F. M. et al., Current Protocols in Molecular Biology, Greene Publishing Associates and Wiley-Interscience, New York, 1987).

[0063] Once the proper assembly of the invention chimeric scFv-INT-1 protein and adhesion to the epitopes in target cell lines, e.g., tumor cell lines, has been tested in a non-pathogenic yeast cell (e.g., Saccharomyces cerevisiae) homologous recombination can be used to insert a polynucleotide sequence encoding the chimeric scFv-INT1 into Candida albicans, and similar ex vivo experiments as those performed for S. cerevisiae will be performed to assure that replacement of the I domain does not seriously impair the proper folding and targeting of scFv-INT1. At this point, ex vivo experiments verifying adhesion of this mutant C. albicans strain to cancer cells are performed, in addition to preliminary in vivo mice experiments to ascertain that this targeting alone is adequate in mice to restrict pathogenicity and targeting to tumors.

[0064] The most common model for human cancers is a murine subject that has been transfected with human carcinomas. After an incubation period varying from weeks to months after carcinoma introduction to allow growth of test tumors, transfected mice will be treated with the genetically modified C. albicans. Survival of the mice and tumor spreading are monitored over time. Biopsies of the tumorous tissues can also be taken to investigate C. albicans invasion. By using large groups of genetically identical mice, aggregate data can be collected.

[0065] Evolution has optimized certain organisms to invade mammalian tissue. The present invention harnesses this powerful and highly pathogenic trait to generate a new weapon against cancer and other diseases characterized by the presence of cells with a disease-associated antigen. In contrast to more indirect methodologies previously applied that recruit the natural immune system responses, fusion scFv-INT1 proteins targeted to disease-associated tissues will direct aggressive invasion of the naturally invasive pathogen to diseased host tissue. The method of the present invention is a novel approach to cancer treatment that recruits the previously untapped resource of pathogenic organisms (e.g. fungi) as potent and specific therapy to eliminate diseased tissue characterized by disease-associated antigens.

[0066] The invention will now be described by reference to the following non-limiting illustrative example:

EXAMPLE 1 Construction of the scFv-INT1 Fusion Gene

[0067] Using bulk genomic DNA from C. albicans, primers 1 and 2 (shown in FIGS. 2A-B) (SEQ ID NOS:2 and 3) are used for PCR amplification of the INT1 gene (available from GenBank under accession number U35070) (SEQ ID NO:1) as previously described (Gale 1996). These primers insert SacI and ApaI restriction sites at the 5′ and 3′ ends of the coding region of INT1, respectively. These restriction sites are both nonexistent in the ORF of the gene (see gene sequence in FIGS. 1A-W). The 5 kB product of this PCR reaction is isolated using a standard Qiagen desalting kit, digested with the appropriate enzymes SacI and ApaI, and ligated into predigested and dephosphorylated pBluescript II SK (+) phagemid plasmid according to the manufacturer's instructions (Product #212205, Stratagene, LaJolla, Calif.). ssDNA incorporating the INT1 gene is then generated using standard techniques with helper phage and uridine in dut⁻ ung⁻ strains of E. Coli according to the manufacturer's instructions.

[0068] To introduce multiple cloning sites in the ssDNA PCR product in the place of the I domain of INT1, primer 7 (shown in FIGS. 2A-B) (SEQ ID NO:8) is used in a standard polymerase/ligase reaction; also thus eliminating the I domain. Isolation of the generated plasmids is performed using standard techniques.

[0069] Single chain antibodies (scFvs) having the target antigen binding region of a desired antigen are generated using reverse transcriptase PCR of the bulk RNA from antibody-generating cell lines using primers 4 to 6 (shown in FIGS. 2A-B) (SEQ ID NOS:5, 6, and 7). The binding regions are subcloned into the cut and dephosphorylated plasmid prepared as described above, and then a fusion gene is isolated and characterized using techniques described in Z. Eshhar et al., Methods in Enzymology 8:133-142 (1995), except that Primers 4 to 6 differ from those shown in Eshhar by including different restriction endonuclease sites, as INT1 has restriction sites for the nucleases used by Eshhar. The primers used to remove the binding regions of the heavy and light chains incorporate a linker that allows the now-assembled scFv-INT1 protein to have the binding region activated and folded properly.

[0070] The chimeric INT1-scFv fusion protein is directly expressed in E. Coli for in vitro studies of folding and binding using known techniques described in Sections 10.0.1 and 16.1 to 16.7 of Current Protocols in Molecular Biology, Collected Volumes 1 to 4, edited by Ausubel, F. M. et al., John Wiley &Sons, 2000. In addition, the chimeric INT1-scFv fusion protein is incorporated into S. Cerevisiae using an expression plasmid containing the nucleotide sequence that encodes the fusion protein for cell-cell studies and is incorporated back into Candida albicans by homologous recombination using techniques described in Section 13.10.3 of Current Protocols in Molecular Biology, supra. Thus, a tumor-specific organism is readily accomplished.

[0071] It will be apparent to those skilled in the art that various changes may be made in the invention without departing from the spirit and scope thereof, and therefore, the invention encompasses embodiments in addition to those specifically disclosed in the specification, but only as indicated in the appended claims.

1 8 1 5194 DNA Candida albicans 1 cccaaaaaag ataaaataaa aacaaaacaa aacaaaagta ctaacaaatt attgaaactt 60 ttaattttta ataaagaatc agtagatcta ttgttaaaag aaatgaactc aactccaagt 120 aaattattac cgatagataa acattctcat ttacaattac agcctcaatc gtcctcggca 180 tcaatattta attccccaac aaaaccattg aatttcccca gaacaaattc caagccgagt 240 ttagatccaa attcaagctc tgatacctac actagcgaac aagatcaaga gaaagggaaa 300 gaagagaaaa aggacacagc ctttcaaaca tcttttgata gaaattttga tcttgataat 360 tcaatcgata tacaacaaac aattcaacat cagcaacaac agccacaaca acaacaacaa 420 ctctcacaaa ccgacaataa tttaattgat gaattttctt ttcaaacacc gatgacttcg 480 actttagacc taaccaagca aaatccaact gtggacaaag tgaatgaaaa tcatgcacca 540 acttatataa atacctcccc caacaaatca ataatgaaaa aggcaactcc taaagcgtca 600 cctaaaaaag ttgcatttac tgtaactaat cccgaaattc atcattatcc agataataga 660 gtcgaggaag aagatcaaag tcaacaaaaa gaagattcag ttgagccacc cttaatacaa 720 catcaatgga aagatccttc tcaattcaat tattctgatg aagatacaaa tgcttcagtt 780 ccaccaacac caccacttca tacgacgaaa cctacttttg cgcaattatt gaacaaaaac 840 aacgaagtca atctggaacc agaggcattg acagatatga aattaaagcg cgaaaatttc 900 agcaatttat cattagatga aaaagtcaat ttatatctta gtcccactaa taataacaat 960 agtaagaatg tgtcagatat ggatctgcat ttacaaaact tgcaagacgc ttcgaaaaac 1020 aaaactaatg aaaatattca caatttgtca tttgctttaa aagcaccaaa gaatgatatt 1080 gaaaacccat taaactcatt gactaacgca gatattctgt taagatcatc tggatcatca 1140 caatcgtcat tacaatcttt gaggaatgac aatcgtgtct tggaatcagt gcctgggtca 1200 cctaagaagg ttaatcctgg attgtctttg aatgacggca taaaggggtt ctctgatgag 1260 gttgttgaat cattacttcc tcgtgactta tctcgagaca aattagagac tacaaaagaa 1320 catgatgcac cagaacacaa caatgagaat tttattgatg ctaaatcgac taataccaat 1380 aagggacaac tcttagtatc atctgatgat catttggact cttttgatag atcctataac 1440 cacactgaac aatcaatttt gaatcttttg aatagtgcat cacaatctca aatttcgtta 1500 aatgcattgg aaaaacaaag gcaaacacag gaacaagaac aaacacaagc ggcagagcct 1560 gaagaagaaa cttcgtttag tgataatatc aaagttaaac aagagccaaa gagcaatttg 1620 gagtttgtca aggttaccat caagaaagaa ccagttctgg ccacggaaat aaaagctcca 1680 aaaagagaat tttcaagtcg aatattaaga ataaaaaatg aagatgaaat tgccgaacca 1740 gctgatattc atcctaaaaa agaaaatgaa gcaaacagtc atgtcgaaga tactgatgca 1800 ttgttgaaga aagcacttaa tgatgatgag gaatctgaca cgacccaaaa ctcaacgaaa 1860 atgtcaattc gttttcatat tgatagtgat tggaaattgg aagacagtaa tgatggcgat 1920 agagaagata atgatgatat ttctcgtttt gagaaatcag atattttgaa cgacgtatca 1980 cagacttctg atattattgg tgacaaatat ggaaactcat caagtgaaat aaccaccaaa 2040 acattagcac ccccaagatc ggacaacaat gacaaggaga attctaaatc tttggaagat 2100 ccagctaata atgaatcatt gcaacaacaa ttggaggtac cgcatacaaa agaagatgat 2160 agcattttag ccaactcgtc caatattgct ccacctgaag aattgacttt gcccgtagtg 2220 gaagcaaatg attattcatc ttttaatgac gtgaccaaaa cttttgatgc atactcaagc 2280 tttgaagagt cattatctag agagcacgaa actgattcaa aaccaattaa tttcatatca 2340 atttggcata aacaagaaaa gcagaagaaa catcaaattc ataaagttcc aactaaacag 2400 atcattgcta gttatcaaca atacaaaaac gaacaagaat ctcgtgttac tagtgataaa 2460 gtgaaaatcc caaatgccat acaattcaag aaattcaaag aggtaaatgt catgtcaaga 2520 agagttgtta gtccagacat ggatgatttg aatgtatctc aatttttacc agaattatct 2580 gaagactctg gatttaaaga tttgaatttt gccaactact ccaataacac caacagacca 2640 agaagtttta ctccattgag cactaaaaat gtcttgtcga atattgataa cgatcctaat 2700 gttgttgaac ctcctgaacc gaaatcatat gctgaaatta gaaatgctag acggttatca 2760 gctaataagg cagcgccaaa tcaggcacca ccattgccac cacaacgaca accatcttca 2820 actcgttcca attcaaataa acgagtgtcc agatttagag tgcccacatt tgaaattaga 2880 agaacttctt cagcattagc accttgtgac atgtataatg atatttttga tgatttcggt 2940 gcgggttcta aaccaactat aaaggcagaa ggaatgaaaa cattgccaag tatggataaa 3000 gatgatgtca agaggatttt gaatgcaaag aaaggtgtga ctcaagatga atatataaat 3060 gccaaacttg ttgatcaaaa acctaaaaag aattcaattg tcaccgatcc cgaagaccga 3120 tatgaagaat tacaacaaac tgcctctata cacaatgcca ccattgattc aagtatttat 3180 ggccgaccag actccatttc taccgacatg ttgccttatc ttagtgatga attgaaaaaa 3240 ccacctacgg ctttattatc tgctgatcgt ttgtttatgg aacaagaagt acatccgtta 3300 agatcaaact ctgttttggt tcacccaggg gcaggagcag caactaattc ttcaatgtta 3360 ccagagccag attttgaatt aatcaattca cctgctagaa atgtgctgaa caacagtgat 3420 aatgtcgcca tcagtggtaa tgctagtact attagtttta accaattgga tatgaatttt 3480 gatgaccaag ctacaattgg tcaaaaaatc caagagcaac ctgcttcaaa atccgccaat 3540 actgttcgtg gtgatgatga tggattggcc agtgcacctg aaacaccaag aactcctacc 3600 aaaaaggagt ccatatcaag caagcctgcc aagctttctt ctgcctcccc tagaaaatca 3660 ccaattaaga ttggttcacc agttcgagtt attaagaaaa atggatcaat tgctggcatt 3720 gaaccaatcc caaaagccac tcacaaaccg aagaaatcat tccaaggaaa cgagatttca 3780 aaccataaag tacgagatgg tggaatttca ccaagctccg gatcagagca tcaacagcat 3840 aatcctagta tggtttctgt tccttcacag tatactgatg ctacttcaac ggttccagat 3900 gaaaacaaag atgttcaaca caagcctcgt gaaaagcaaa agcaaaagca tcaccatcgc 3960 catcatcatc atcatcataa acaaaaaact gatattccgg gtgttgttga tgatgaaatt 4020 cctgatgtag gattacaaga acgaggcaaa ttattcttta gagttttagg aattaagaat 4080 atcaatttac ccgatattaa tactcacaaa ggaagattca ctttaacgtt ggataatgga 4140 gtgcattgtg ttactacacc agaatacaac atggacgacc ataatgttgc cataggtaaa 4200 gaatttgagt tgacagttgc tgattcatta gagtttattt taactttgaa ggcatcatat 4260 gaaaaacctc gtggtacatt agtagaagtg actgaaaaga aagttgtcaa atcaagaaat 4320 agattgagtc gattatttgg atcgaaagat attatcacca cgacaaagtt tgtgcccact 4380 gaagtcaaag atacctgggc taataagttt gctcctgatg gttcatttgc tagatgttac 4440 attgatttac aacaatttga agaccaaatc accggtaaag catcacagtt tgatctcaat 4500 tgttttaatg aatgggaaac tatgagtaat ggcaatcaac caatgaaaag aggcaaacct 4560 tataagattg ctcaattgga agttaaaatg ttgtatgttc cacgatcaga tccaagagaa 4620 atattaccaa ccagcattag atccgcatat gaaagcatca atgaattaaa caatgaacag 4680 aataattact ttgaaggtta tttacatcaa gaaggaggtg attgtccaat ttttaagaaa 4740 cgttttttca aattaatggg cacttcttta ttggctcata gtgaaatatc tcataaaact 4800 agagccaaaa ttaatttatc aaaagttgtt gatttgattt atgttgataa agaaaacatt 4860 gatcgttcca atcatcgaaa tttcagtgat gtgttattgt tggatcatgc attcaaaatc 4920 aaatttgcta atggtgagtt gattgatttt tgtgctccta ataaacatga aatgaaaata 4980 tggattcaaa atttacaaga aattatctat agaaatcggt tcagacgtca accatgggta 5040 aatttgatgc ttcaacaaca acaacaacaa caacaacaac aaagctccca acagtaattg 5100 aaaggtctac ttttgatttt tttaatttta attggcaaat atatgcccat tttgtattat 5160 cttttagtct aatagcgttt tctttttttc cagt 5194 2 40 DNA Artificial sequence PCR primer 2 cgctatagag ctcaattttt aataaagaat cagtagatct 40 3 45 DNA Artificial sequence PCR primer 3 agcgtatagg gcccgagata atacaaaatg ggcatatatt tgcca 45 4 37 DNA Artificial sequence PCR primer 4 cccgtctaga ggagayatyg twatgaccca gtctcca 37 5 32 DNA Artificial sequence PCR primer 5 cccgtcgacc ctttwaattc cagcttwgts cc 32 6 66 DNA Artificial sequence PCR primer 6 cgggtcgact tccggtagcg gcaaatcctc tgaaggcaaa ggtsaggtsc agctgsagsa 60 gtctgg 66 7 33 DNA Artificial sequence PCR primer 7 tgmrgagacg gatccgtrgt yccttggccc cag 33 8 72 DNA Artificial sequence PCR primer 8 ttgttcttgt tcctgtgttt gcctttgcgg ccgatcgcag gatcctggaa ctgaagcatt 60 tgtatcttca tc 72 

What is claimed is:
 1. A chimeric pathogenic organism wherein virulent transformation of the organism is controlled in the wild-type organism by binding of the I domain of a surface integrin-like protein to a cell, said chimeric organism comprising a chimeric surface integrin-like fusion protein in which the I domain is replaced by an antibody fragment that binds a disease-associated antigen on a cell, wherein binding of the antibody fragment to the disease-associated antigen triggers virulent transformation of the chimeric pathogenic organism so as to cause the organism to infiltrate the cell.
 2. The chimeric pathogenic organism of claim 1, wherein the antibody fragment is a single chain antibody.
 3. The chimeric pathogenic organism of claim 1, wherein the antibody fragment binds to an antigen on a tumor cell.
 4. The chimeric pathogenic organism of claim 3, wherein the antigen is contained in an abnormal surface protein of the tumor cell.
 5. The chimeric pathogenic organism of claim 3, wherein the antigen is selected from the group consisting of GAG-72, ERBB2, EGP-2, CEA, CD44, I-FR, neu, and the Lewis (Y) tumor associated antigen.
 6. The chimeric pathogenic organism of claim 3, wherein the tumor cell is selected from the group consisting of adenocarcinoma of colon, ovary or breast; cervical nonmucinous ovarian carcinoma; and breast, ovarian , colorectal, and pancreatic cancers.
 7. A chimeric pathogenic C. albicans comprising: an integrinl (INT1) fusion protein in which the I domain is replaced by an antibody fragment that binds to a disease-associated antigen on a diseased cell, a disabled wild-type high affininity iron transporter (CAFTR) gene, and a DNA construct comprising a wild-type CAFTR gene under the control of an enhanced filamentous growth protein (EFG1p) response element, wherein binding of the antibody to the disease-associated antigen triggers expression of the CAFTR gene in the DNA construct and filamentous transformation in the chimeric pathogenic C albicans.
 8. The chimeric pathogenic C. Albicans of claim 7, wherein the antibody fragment is a single chain antibody.
 9. The chimeric pathogenic C. Albicans of claim 7, wherein the antibody fragment binds to an antigen on a tumor cell.
 10. The chimeric pathogenic C. Albicans of claim 9, wherein the antigen is contained in an abnormal surface protein of the tumor cell.
 11. The chimeric pathogenic C. Albicans of claim 9, wherein the antigen is selected from the group consisting of GAG-72, ERBB2, EGP-2, CEA, CD44, I-FR, neu, and the Lewis (Y) tumor associated antigen.
 12. The chimeric pathogenic C. Albicans of claim 9, wherein the tumor cell is selected from the group consisting of adenocarcinoma of colon, ovary or breast; cervical nonmucinous ovarian carcinoma; and breast, ovarian, colorectal, and pancreatic cancers.
 13. A method for treating a disease associated with the presence of cells having a disease-associated surface antigen in a subject in need thereof, said method comprising: administering to the subject a therapeutically effective amount of a chimeric pathogenic organism according to claim 1 so as to cause binding of the antibody fragment to the disease-associated antigen on the cells, thereby treating the disease by triggering infiltration of the chimeric pathogenic organism into the cells without substantial damage to healthy cells.
 14. The method of claim 13, wherein the antibody fragment is a single chain antibody.
 15. The method of claim 13, wherein the antibody fragment binds to an antigen on a tumor cell.
 16. The method of claim 15, wherein the disease-associated antigen is contained in an abnormal surface protein of the tumor cell.
 17. The method of claim 16, wherein the antigen is selected from the group consisting of GAG-72, ERBB2, EGP-2, CEA, CD44, I-FR, neu, and the Lewis (Y) tumor associated antigen.
 18. The method of claim 15, wherein the tumor cell is selected from the group consisting of adenocarcinoma of colon, ovary or breast; cervical nonmucinous ovarian carcinoma; and breast, ovarian , colorectal, and pancreatic cancers.
 19. The method of claim 15, wherein the antigen is a tumor marker.
 20. The method of claim 19, wherein the method further comprises administering to the subject a therapeutic amount of an immunosuppressive agent.
 21. The method of claim 20, wherein the immunosuppressive agent is selected from the group consisting of cyclosporin A, OKT3, FK506, mycophenolate mofetil (MMF), azathioprine, a corticosteroid, an antilymphocyte globulin, and an antithymocyte globulin.
 22. A method for generating a chimeric therapeutic organism from a pathogenic organism that possesses in the wild-type an integrin-like protein with an I domain, said method comprising: replacing the I domain in the integrin-like protein of the pathogenic organism with an antibody fragment that binds to a disease-associated antigen on a diseased cell; wherein the wild-type pathogenic organism undergoes virulent transformation by binding of the I domain of the surface integrin-like protein to a cell, and wherein the chimeric therapeutic organism undergoes virulent transformation by binding of the antibody fragment to the disease-associated antigen on the cell.
 23. The method of claim 22, wherein the pathogenic organism is C. albicans and wherein the method further comprises disabling the wild-type CAFTR gene in the C. albicans, and introducing a DNA construct comprising a wild-type CAFTR gene under the control of a EFG1p response element, wherein binding of the antibody fragment to the disease-associated antigen triggers expression of the CAFTR gene in the DNA construct and filamentous transformation in the chimeric pathogenic C. albicans.
 24. The method of claim 23, wherein the antibody fragment is a single chain antibody.
 25. The method of claim 23, wherein the antibody fragment binds to an antigen on a tumor cell.
 26. The method of claim 25, wherein the disease-associated antigen is contained in an abnormal surface protein of the tumor cell. 